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Cancer Cell‐Specific Fluorescent Prodrug Delivery Platforms

Targeting cancer cells with high specificity is one of the most essential yet challenging goals of tumor therapy. Because different surface receptors, transporters, and integrins are overexpressed specifically on tumor cells, using these tumor cell‐specific properties to improve drug targeting effic...

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Autores principales: Ma, Siyue, Kim, Ji Hyeon, Chen, Wei, Li, Lu, Lee, Jieun, Xue, Junlian, Liu, Yuxia, Chen, Guang, Tang, Bo, Tao, Wei, Kim, Jong Seung
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10238224/
https://www.ncbi.nlm.nih.gov/pubmed/37026629
http://dx.doi.org/10.1002/advs.202207768
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author Ma, Siyue
Kim, Ji Hyeon
Chen, Wei
Li, Lu
Lee, Jieun
Xue, Junlian
Liu, Yuxia
Chen, Guang
Tang, Bo
Tao, Wei
Kim, Jong Seung
author_facet Ma, Siyue
Kim, Ji Hyeon
Chen, Wei
Li, Lu
Lee, Jieun
Xue, Junlian
Liu, Yuxia
Chen, Guang
Tang, Bo
Tao, Wei
Kim, Jong Seung
author_sort Ma, Siyue
collection PubMed
description Targeting cancer cells with high specificity is one of the most essential yet challenging goals of tumor therapy. Because different surface receptors, transporters, and integrins are overexpressed specifically on tumor cells, using these tumor cell‐specific properties to improve drug targeting efficacy holds particular promise. Targeted fluorescent prodrugs not only improve intracellular accumulation and bioavailability but also report their own localization and activation through real‐time changes in fluorescence. In this review, efforts are highlighted to develop innovative targeted fluorescent prodrugs that efficiently accumulate in tumor cells in different organs, including lung cancer, liver cancer, cervical cancer, breast cancer, glioma, and colorectal cancer. The latest progress and advances in chemical design and synthetic considerations in fluorescence prodrug conjugates and how their therapeutic efficacy and fluorescence can be activated by tumor‐specific stimuli are reviewed. Additionally, novel perspectives are provided on strategies behind engineered nanoparticle platforms self‐assembled from targeted fluorescence prodrugs, and how fluorescence readouts can be used to monitor the position and action of the nanoparticle‐mediated delivery of therapeutic agents in preclinical models. Finally, future opportunities for fluorescent prodrug‐based strategies and solutions to the challenges of accelerating clinical translation for the treatment of organ‐specific tumors are proposed.
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spelling pubmed-102382242023-06-04 Cancer Cell‐Specific Fluorescent Prodrug Delivery Platforms Ma, Siyue Kim, Ji Hyeon Chen, Wei Li, Lu Lee, Jieun Xue, Junlian Liu, Yuxia Chen, Guang Tang, Bo Tao, Wei Kim, Jong Seung Adv Sci (Weinh) Reviews Targeting cancer cells with high specificity is one of the most essential yet challenging goals of tumor therapy. Because different surface receptors, transporters, and integrins are overexpressed specifically on tumor cells, using these tumor cell‐specific properties to improve drug targeting efficacy holds particular promise. Targeted fluorescent prodrugs not only improve intracellular accumulation and bioavailability but also report their own localization and activation through real‐time changes in fluorescence. In this review, efforts are highlighted to develop innovative targeted fluorescent prodrugs that efficiently accumulate in tumor cells in different organs, including lung cancer, liver cancer, cervical cancer, breast cancer, glioma, and colorectal cancer. The latest progress and advances in chemical design and synthetic considerations in fluorescence prodrug conjugates and how their therapeutic efficacy and fluorescence can be activated by tumor‐specific stimuli are reviewed. Additionally, novel perspectives are provided on strategies behind engineered nanoparticle platforms self‐assembled from targeted fluorescence prodrugs, and how fluorescence readouts can be used to monitor the position and action of the nanoparticle‐mediated delivery of therapeutic agents in preclinical models. Finally, future opportunities for fluorescent prodrug‐based strategies and solutions to the challenges of accelerating clinical translation for the treatment of organ‐specific tumors are proposed. John Wiley and Sons Inc. 2023-04-07 /pmc/articles/PMC10238224/ /pubmed/37026629 http://dx.doi.org/10.1002/advs.202207768 Text en © 2023 The Authors. Advanced Science published by Wiley‐VCH GmbH https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Reviews
Ma, Siyue
Kim, Ji Hyeon
Chen, Wei
Li, Lu
Lee, Jieun
Xue, Junlian
Liu, Yuxia
Chen, Guang
Tang, Bo
Tao, Wei
Kim, Jong Seung
Cancer Cell‐Specific Fluorescent Prodrug Delivery Platforms
title Cancer Cell‐Specific Fluorescent Prodrug Delivery Platforms
title_full Cancer Cell‐Specific Fluorescent Prodrug Delivery Platforms
title_fullStr Cancer Cell‐Specific Fluorescent Prodrug Delivery Platforms
title_full_unstemmed Cancer Cell‐Specific Fluorescent Prodrug Delivery Platforms
title_short Cancer Cell‐Specific Fluorescent Prodrug Delivery Platforms
title_sort cancer cell‐specific fluorescent prodrug delivery platforms
topic Reviews
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10238224/
https://www.ncbi.nlm.nih.gov/pubmed/37026629
http://dx.doi.org/10.1002/advs.202207768
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